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Tacrolimus

NDC 67877-280 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203740
Dosage form / routeCAPSULE · ORAL
Active ingredientsTACROLIMUS (5 mg/1)
Marketing started20201113
Package count2

External sources

Source: openFDA. Public-domain (CC0).